G.M. Lathrop

44.7k citations

235 papers · 16.2k indexed · 7 hit papers · h-index 56

Impact in

Genetics top 0.05%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Diabetes and associated disorders
Molecular Biology top 0.5%

Papers in

Genetics 110
- Genomic variations and chromosomal abnormalities 46
- Genetic Mapping and Diversity in Plants and Animals 25
- Genetic Associations and Epidemiology 20
Molecular Biology 113
- DNA and Nucleic Acid Chemistry 53
- DNA Repair Mechanisms 30
- Genomics and Chromatin Dynamics 16
- RNA and protein synthesis mechanisms 12

Co-authors: J.-M. Lalouel Cécile Julier J Ott Jürg Ott P. O’Connell Yusuke Nakamura Marc Délepine William Cookson
Journals: Nucleic Acids Research (115 papers)Genomics (13 papers)Nature Genetics (12 papers)Nature (6 papers)Proceedings of the National Academy of Sciences (6 papers)
Partner nations: United States France United Kingdom

In The Last Decade

G.M. Lathrop

235 papers receiving 15.7k citations

Hit Papers

7 papers align trajectories log scale

A genome-wide association study of global gene expression 2007 · 632 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2007 Nature Genetics
2000 Nature Genetics
1996 Nature
1996 Nature Genetics
1985 PubMed
1984 Proceedings of the National Academy of Sciences
1984 PubMed

Peers

Countries citing papers authored by G.M. Lathrop

Since Specialization

Citations

This map shows the geographic impact of G.M. Lathrop's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by G.M. Lathrop with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G.M. Lathrop more than expected).

Fields of papers citing papers by G.M. Lathrop

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G.M. Lathrop. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by G.M. Lathrop. The network helps show where G.M. Lathrop may publish in the future.

Co-authors

The 25 scholars most cited alongside G.M. Lathrop, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with G.M. Lathrop Line = papers co-authored together G.M. Lathrop links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study European Respiratory Journal ·Tomoko Nakanishi, Agustin Cerani, Vincenzo Forgetta, Sirui Zhou, Richard J. Allen, Olivia C. Leavy, Masaru Koido, Deborah Assayag, Gísli Jenkins, Louise V. Wain, Ivana V. Yang, G.M. Lathrop, Paul J. Wolters, David A. Schwartz, J. Brent Richards	2021	12
2	A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines Genome Research ·Liming Liang, Nilesh Morar, Anna Dixon, G.M. Lathrop, Gonçalo R. Abecasis, Miriam F. Moffatt, William Cookson	2013	91
3	Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension The American Journal of Human Genetics ·Chris Wallace, Mingzhan Xue, Stephen Newhouse, Ana Carolina B. Marçano, Abiodun Onipinla, Beverley Burke, Johannie Gungadoo, Richard Dobson, Morris J. Brown, John Connell, Anna F. Dominiczak, G.M. Lathrop, John Webster, Martin Farrall, Charles A. Mein, Nilesh J. Samani, Mark J. Caulfield, David Clayton, Patricia B. Munroe	2006	21
4	Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study. Hypertension ·Patricia B. Munroe, Chris Wallace, Charles A. Mein, Richard Dobson, Mei Xue, Mingxiao Xu, Beverley Burke, Johannie Gungadoo, Abiodun Onipinla, Stephen Newhouse, J Pembroke, J Connell, Marc D. Brown, N. J. Samani, Agung Prija Utama, Jennifer Webster, G.M. Lathrop, D Clayton, Martin Farrall, Mark J. Caulfield	2005	1
5	Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study Human Molecular Genetics ·Stephen Newhouse, Chris Wallace, Richard Dobson, Charles A. Mein, J Pembroke, Martin Farrall, David Clayton, Morris J. Brown, Nilesh J. Samani, Anna F. Dominiczak, John Connell, John Webster, G.M. Lathrop, Mark J. Caulfield, Patricia B. Munroe	2005	69
6	A Gene-Based Genetic Linkage and Comparative Map of the Rat X Chromosome Genomics ·Iona Y. Millwood, Marie‐Thérèse Bihoreau, Dominique Gauguier, M Vinci, Elaine R. Levy, Reinhold Kreutz, G.M. Lathrop, Anthony P. Monaco	1997	40
7	A pharmacogenetic approach to blood pressure in Lyon hypertensive rats. A chromosome 2 locus influences the response to a calcium antagonist. Journal of Clinical Investigation ·M. Vincent, Nilesh J. Samani, Dominique Gauguier, John R. Thompson, G.M. Lathrop, J Sassard	1997	35
8	Polygenic control of autoimmune diabetes in nonobese diabetic mice Nature Genetics ·Soumitra Ghosh, Sheila Palmer, Nanda R. Rodrigues, Heather J. Cordell, Catherine M. Hearne, Richard J. Cornall, Jan‐Bas Prins, PE McShane, G.M. Lathrop, L. Peterson, Linda S. Wicker, John A. Todd	1993	251
9	Rat gene mapping using PCR-analyzed microsatellites. Genetics ·T. Serikawa, Takashi Kuramoto, Pascale Hilbert, Masayuki Mori, Junzo Yamada, Christopher Dubay, David J. Jörg, Detlev Ganten, Jean‐Louis Guénet, G.M. Lathrop	1992	304
10	Isolation and mapping of a polymorphic DNA sequence (HBI18P1) on chromosome 11 [D11S147] Nucleic Acids Research ·Cécile Julier, Yusuke Nakamura, G.M. Lathrop, J.-M. Lalouel, R. White	1989	2
11	Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57] Nucleic Acids Research ·Yusuke Nakamura, Melanie Culver, Brian V. Jensen, M. Leppert, P. O’Connell, G.M. Lathrop, J.-M. Lalouel, R. White	1988	30
12	Isolation and mapping of a polymorphic DNA sequence (cYNA4) on chromosome 2 (D2S50) Nucleic Acids Research ·Yusuke Nakamura, E. Fujimoto, P. O’Connell, M. Leppert, G.M. Lathrop, J.-M. Lalouel, R. White	1988	1
13	Isolation and mapping of a polymorphic DNA sequence (pYNH3) on chromosome X [DXS287] Nucleic Acids Research ·Yusuke Nakamura, L. Ballard, M. Leppert, P. O’Connell, G.M. Lathrop, J.-M. Lalouel, R. White	1988	5
14	A mapped set of DNA markers for human chromosome 17 Genomics ·Yusuke Nakamura, G.M. Lathrop, P. O’Connell, (unknown), David Barker, E Wright, (unknown), Ratna Pancawati, M. Litt, (unknown), (unknown)	1988	127
15	Isolation and mapping of a polymorphic DNA sequence (pEFD6) on chromosome 6 (D6S41) Nucleic Acids Research ·Yusuke Nakamura, E. Fujimoto, M. Leppert, 坂本正裕, G.M. Lathrop, J.-M. Lalouel, R. White	1988	1
16	Isolation and mapping of a polymorphic DNA sequence cEFD52 on chromosome 17q [D17S26] Nucleic Acids Research ·Yusuke Nakamura, E. Fujimoto, P. O’Connell, M. Leppert, G.M. Lathrop, J.-M. Lalouel, R. White	1988	6
17	Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23] Nucleic Acids Research ·E. Fujimoto, Yusuke Nakamura, Serdar SelÃ§uk, P. O’Connell, M. Leppert, G.M. Lathrop, J.-M. Lalouel, R. White	1988	2
18	Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15 [Dl5S38] Nucleic Acids Research ·E. Fujimoto, Yusuke Nakamura, L. Ballard, P. O’Connell, M. Leppert, G.M. Lathrop, Jean-Marc Lalouel, R. White	1988	3
19	Isolation and mapping of a polymorphic DNA sequence pHHH122 on chromosome 2 (D2S54) Nucleic Acids Research ·E. Fujimoto, Yusuke Nakamura, P. O’Connell, M. Leppert, G.M. Lathrop, Jean-Marc Lalouel, R. White	1987	3
20	Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S10) Nucleic Acids Research ·M. Carlson, Yusuke Nakamura, K. Krapcho, E. Fujimoto, P. O’Connell, M. Leppert, G.M. Lathrop, Jean-Marc Lalouel, R. White	1987	7

About G.M. Lathrop

G.M. Lathrop is a scholar working on Genetics, Molecular Biology, Hematology, Physiology and Immunology, having authored 235 papers that have together received 16.2k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (53 papers), Genomic variations and chromosomal abnormalities (46 papers), DNA Repair Mechanisms (30 papers), Genetic Mapping and Diversity in Plants and Animals (25 papers), Genetic Associations and Epidemiology (20 papers), Genomics and Chromatin Dynamics (16 papers), RNA and protein synthesis mechanisms (12 papers) and Chromosomal and Genetic Variations (12 papers). The work is most often cited by research in Genetics (7.1k citations), Molecular Biology (6.7k citations), Immunology (1.9k citations), Immunology and Allergy (544 citations) and Cell Biology (1.2k citations). G.M. Lathrop has collaborated with scholars based in United States, France and United Kingdom. Frequent co-authors include J.-M. Lalouel, Cécile Julier, J Ott, Jürg Ott, P. O’Connell, Yusuke Nakamura, Marc Délepine, William Cookson, M. Leppert and R. White. Their work appears in journals such as Nucleic Acids Research, Genomics, Nature Genetics, Nature and Proceedings of the National Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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